Senior Clinical Field Specialist

JR United Kingdom; Cheltenham; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading company in medical device development seeks a Senior Clinical Field Specialist in Cheltenham. This role involves managing clinical trials, training staff on device usage, ensuring compliance, and supporting case activities. Ideal candidates will have relevant degrees and experience in clinical research, along with strong organizational and communication skills.

Qualifications

• Bachelor’s degree in a relevant field; master’s preferred.
• Experience as Clinical Research Associate, Clinical Specialist, or similar.
• Knowledge of GCP, ISO14155, ICH guidelines.

Responsibilities

• Train study staff on correct use of the device.
• Manage clinical trial activities from initiation to close-out.
• Ensure accurate data collection and resolve discrepancies.

Skills

Organizational Skills

Communication Skills

Knowledge of GCP

Knowledge of ISO14155

Knowledge of ICH Guidelines

Education

Bachelor’s degree in a relevant field

Master’s degree (preferred)

Tools

CTMS software

EDC software

Job description

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Senior Clinical Field Specialist, Cheltenham

Client: The Mullings Group

Location: Cheltenham

Job Category: Other

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EU work permit required: Yes

Job Views: 6

Posted: 26.06.2025

Expiry Date: 10.08.2025

Job Description:

In recent decades, treatment of heart attacks by minimally invasive percutaneous coronary intervention (PCI) has significantly improved patient outcomes. However, successful re-opening of narrow or blocked coronary arteries does not always restore blood flow to the entire heart muscle.

Our client is developing a first-in-class medical device that will diagnose MVO in real-time during PCI and serve as a treatment platform in the cath lab.

As they roll out their clinical trial across Europe, we are hiring a Senior Clinical Research Specialist to oversee and manage clinical trials, support proctoring activities, and take on advanced responsibilities.

Responsibilities:

• Proctoring and Case Support Duties:
• Train study staff on the correct use of the device.
• Supervise site workflow setup to ensure quality data collection.
• Maintain proctoring records and documentation.
• Support site staff during live cases.
• Authorize independent use of the device at clinical sites.
• Join clinical cases to support device use.

• Clinical Trial Support:
• Manage clinical trial activities from initiation to close-out.
• Train and educate site staff on study procedures and software.
• Conduct site visits to ensure compliance and data integrity.
• Collaborate with investigators and CROs.

• Regulatory Requirements Support:
• Assist with IRB submissions and audits.

• Data Management:
• Ensure accurate data collection and resolve discrepancies.

Qualifications:

• Bachelor’s degree in a relevant field; master’s preferred.
• Experience as Clinical Research Associate, Clinical Specialist, or similar.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Experience in proctoring and site management preferred.
• Strong organizational and communication skills.
• Proficiency in CTMS and EDC software.